Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.

Wincent, J; Bruno, D L; van Bon, B W M; Bremer, A; Stewart, H; Bongers, E M H F; Ockeloen, C W; Willemsen, M H; Keays, D D A; Baird, G; Newbury, D F; Kleefstra, T; Marcelis, C; Kini, U; Stark, Z; Savarirayan, R; Sheffield, L J; Zuffardi, O; Slater, H R; de Vries, B B; Knight, S J L; Anderlid, B-M; Schoumans, J

Wincent, J; Bruno, D L; van Bon, B W M; Bremer, A; Stewart, H; Bongers, E M H F; Ockeloen, C W; Willemsen, M H; Keays, D D A; Baird, G; Newbury, D F; Kleefstra, T; Marcelis, C; Kini, U; Stark, Z; Savarirayan, R; Sheffield, L J; Zuffardi, O; Slater, H R; de Vries, B B; Knight, S J L; Anderlid, B-M; Schoumans, J.

Affiliation

Wincent J; Clinical Genetics Unit, Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

Mol Syndromol ; 1(5): 246-254, 2010.

Article in En | MEDLINE | ID: mdl-22140377

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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Syndromol Year: 2010 Document type: Article Affiliation country:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Syndromol Year: 2010 Document type: Article Affiliation country: